• 文献检索
  • 文档翻译
  • 深度研究
  • 学术资讯
  • Suppr Zotero 插件Zotero 插件
  • 邀请有礼
  • 套餐&价格
  • 历史记录
应用&插件
Suppr Zotero 插件Zotero 插件浏览器插件Mac 客户端Windows 客户端微信小程序
定价
高级版会员购买积分包购买API积分包
服务
文献检索文档翻译深度研究API 文档MCP 服务
关于我们
关于 Suppr公司介绍联系我们用户协议隐私条款
关注我们

Suppr 超能文献

核心技术专利:CN118964589B侵权必究
粤ICP备2023148730 号-1Suppr @ 2026

文献检索

告别复杂PubMed语法,用中文像聊天一样搜索,搜遍4000万医学文献。AI智能推荐,让科研检索更轻松。

立即免费搜索

文件翻译

保留排版,准确专业,支持PDF/Word/PPT等文件格式,支持 12+语言互译。

免费翻译文档

深度研究

AI帮你快速写综述,25分钟生成高质量综述,智能提取关键信息,辅助科研写作。

立即免费体验

细胞在材料驱动的纤连蛋白微环境上的迁移。

Cell migration on material-driven fibronectin microenvironments.

作者信息

Grigoriou E, Cantini M, Dalby M J, Petersen A, Salmeron-Sanchez M

机构信息

Division of Biomedical Engineering, School of Engineering, University of Glasgow, Glasgow, UK.

出版信息

Biomater Sci. 2017 Jun 27;5(7):1326-1333. doi: 10.1039/c7bm00333a.

DOI:10.1039/c7bm00333a
PMID:28612879
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC5858633/
Abstract

Cell migration is a fundamental process involved in a wide range of biological phenomena. However, how the underlying mechanisms that control migration are orchestrated is not fully understood. In this work, we explore the migratory characteristics of human fibroblasts using different organisations of fibronectin (FN) triggered by two chemically similar surfaces, poly(ethyl acrylate) (PEA) and poly(methyl acrylate) (PMA); cell migration is mediated via an intermediate layer of fibronectin (FN). FN is organised into nanonetworks upon simple adsorption on PEA whereas a globular conformation is observed on PMA. We studied cell speed over the course of 24 h and the morphology of focal adhesions in terms of area and length. Additionally, we analysed the amount of cell-secreted FN as well as FN remodelling. Velocity of human fibroblasts was found to exhibit a biphasic behaviour on PEA, whereas it remained fairly constant on PMA. FA analysis revealed more mature focal adhesions on PEA over time contrary to smaller FAs found on PMA. Finally, human fibroblasts seemed to remodel adsorbed FN more on PMA than on PEA. Overall, these results indicate that the cell-protein-material interface affects cell migratory behaviour. Analysis of FAs together with FN secretion and remodelling were associated with differences in cell velocity providing insights into the factors that can modulate cell motility.

摘要

细胞迁移是一个涉及广泛生物现象的基本过程。然而,控制迁移的潜在机制是如何协调的,目前尚未完全了解。在这项工作中,我们利用由两种化学性质相似的表面,即聚丙烯酸乙酯(PEA)和聚丙烯酸甲酯(PMA)引发的不同纤连蛋白(FN)组装形式,来探究人类成纤维细胞的迁移特性;细胞迁移是通过纤连蛋白(FN)的中间层介导的。FN在简单吸附于PEA时会组装成纳米网络,而在PMA上则呈现球状构象。我们研究了24小时内细胞的速度以及粘着斑在面积和长度方面的形态。此外,我们分析了细胞分泌的FN量以及FN的重塑情况。发现人类成纤维细胞在PEA上的速度呈现双相行为,而在PMA上则保持相当恒定。粘着斑分析显示,随着时间推移,PEA上的粘着斑比PMA上的粘着斑更成熟。最后,人类成纤维细胞似乎在PMA上比在PEA上更能重塑吸附的FN。总体而言,这些结果表明细胞 - 蛋白质 - 材料界面会影响细胞的迁移行为。对粘着斑的分析以及FN的分泌和重塑与细胞速度的差异相关,这为能够调节细胞运动性的因素提供了见解。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/d6b1/5858633/cfcda4d4ead1/c7bm00333a-f5.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/d6b1/5858633/edbc8ba23397/c7bm00333a-f1.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/d6b1/5858633/9b51700408b4/c7bm00333a-f2.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/d6b1/5858633/54207480ff46/c7bm00333a-f3.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/d6b1/5858633/847a1560a5cd/c7bm00333a-f4.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/d6b1/5858633/cfcda4d4ead1/c7bm00333a-f5.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/d6b1/5858633/edbc8ba23397/c7bm00333a-f1.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/d6b1/5858633/9b51700408b4/c7bm00333a-f2.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/d6b1/5858633/54207480ff46/c7bm00333a-f3.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/d6b1/5858633/847a1560a5cd/c7bm00333a-f4.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/d6b1/5858633/cfcda4d4ead1/c7bm00333a-f5.jpg

相似文献

1
Cell migration on material-driven fibronectin microenvironments.细胞在材料驱动的纤连蛋白微环境上的迁移。
Biomater Sci. 2017 Jun 27;5(7):1326-1333. doi: 10.1039/c7bm00333a.
2
The strength of the protein-material interaction determines cell fate.蛋白质-材料相互作用的强度决定了细胞命运。
Acta Biomater. 2018 Sep 1;77:74-84. doi: 10.1016/j.actbio.2018.07.016. Epub 2018 Jul 10.
3
Controlled Assembly of Fibronectin Nanofibrils Triggered by Random Copolymer Chemistry.由无规共聚物化学引发的纤连蛋白纳米原纤维的可控组装
ACS Appl Mater Interfaces. 2015 Aug 19;7(32):18125-35. doi: 10.1021/acsami.5b05466. Epub 2015 Aug 10.
4
Effect of topological cues on material-driven fibronectin fibrillogenesis and cell differentiation.拓扑线索对材料驱动的纤连蛋白纤维生成和细胞分化的影响。
J Mater Sci Mater Med. 2012 Jan;23(1):195-204. doi: 10.1007/s10856-011-4532-z. Epub 2011 Dec 27.
5
A material-based platform to modulate fibronectin activity and focal adhesion assembly.一种用于调节纤连蛋白活性和粘着斑组装的基于材料的平台。
Biores Open Access. 2014 Dec 1;3(6):286-96. doi: 10.1089/biores.2014.0033.
6
Vitronectin alters fibronectin organization at the cell-material interface.玻璃连蛋白改变细胞-材料界面处的纤连蛋白组织。
Colloids Surf B Biointerfaces. 2013 Nov 1;111:618-25. doi: 10.1016/j.colsurfb.2013.07.016. Epub 2013 Jul 12.
7
Engineered microenvironments for synergistic VEGF - Integrin signalling during vascularization.血管生成过程中用于协同VEGF-整合素信号传导的工程化微环境
Biomaterials. 2017 May;126:61-74. doi: 10.1016/j.biomaterials.2017.02.024. Epub 2017 Feb 21.
8
Biological activity of the substrate-induced fibronectin network: insight into the third dimension through electrospun fibers.底物诱导的纤连蛋白网络的生物活性:通过电纺纤维洞察三维空间
Langmuir. 2009 Sep 15;25(18):10893-900. doi: 10.1021/la9012203.
9
Role of material-driven fibronectin fibrillogenesis in protein remodeling.物质驱动的纤连蛋白原纤维形成在蛋白质重塑中的作用。
Biores Open Access. 2013 Oct;2(5):364-73. doi: 10.1089/biores.2013.0017.
10
Molecular assembly and biological activity of a recombinant fragment of fibronectin (FNIII(7-10)) on poly(ethyl acrylate).纤维连接蛋白(FNIII(7-10))重组片段在聚丙烯酸乙酯上的分子组装和生物活性
Colloids Surf B Biointerfaces. 2010 Jul 1;78(2):310-6. doi: 10.1016/j.colsurfb.2010.03.019. Epub 2010 Mar 29.

引用本文的文献

1
Engineered Biomimetic Fibrillar Fibronectin Matrices Regulate Cell Adhesion Initiation, Migration, and Proliferation via α5β1 Integrin and Syndecan-4 Crosstalk.工程仿生原纤维纤维连接蛋白基质通过α5β1 整联蛋白和 syndecan-4 串话调节细胞黏附起始、迁移和增殖。
Adv Sci (Weinh). 2023 Aug;10(24):e2300812. doi: 10.1002/advs.202300812. Epub 2023 Jun 25.
2
Epithelial-Mesenchymal Transition Induced in Cancer Cells by Adhesion to Type I Collagen.癌细胞与 I 型胶原黏附诱导的上皮-间充质转化。
Int J Mol Sci. 2022 Dec 22;24(1):198. doi: 10.3390/ijms24010198.
3
Nanofibrous scaffolds for regenerative endodontics treatment.

本文引用的文献

1
Material-driven fibronectin assembly for high-efficiency presentation of growth factors.基于材料的纤连蛋白组装用于高效展示生长因子。
Sci Adv. 2016 Aug 26;2(8):e1600188. doi: 10.1126/sciadv.1600188. eCollection 2016 Aug.
2
Substrate engagement of integrins α5β1 and αvβ3 is necessary, but not sufficient, for high directional persistence in migration on fibronectin.整合素α5β1和αvβ3与底物的结合对于在纤连蛋白上迁移时的高定向持续性是必要的,但并不充分。
Sci Rep. 2016 Mar 18;6:23258. doi: 10.1038/srep23258.
3
Lateral Chain Length in Polyalkyl Acrylates Determines the Mobility of Fibronectin at the Cell/Material Interface.
用于再生牙髓治疗的纳米纤维支架
Front Bioeng Biotechnol. 2022 Dec 12;10:1078453. doi: 10.3389/fbioe.2022.1078453. eCollection 2022.
4
Novel synthesis of fibronectin derived photoluminescent carbon dots for bioimaging applications.用于生物成像应用的纤连蛋白衍生光致发光碳点的新型合成方法。
RSC Adv. 2022 Oct 26;12(47):30487-30494. doi: 10.1039/d2ra05137k. eCollection 2022 Oct 24.
5
Bio-functionalization and in-vitro evaluation of titanium surface with recombinant fibronectin and elastin fragment in human mesenchymal stem cell.人骨髓间充质干细胞中重组纤维连接蛋白和弹性蛋白片段对钛表面的生物功能化及体外评估
PLoS One. 2021 Dec 16;16(12):e0260760. doi: 10.1371/journal.pone.0260760. eCollection 2021.
6
Harnessing biomolecules for bioinspired dental biomaterials.利用生物分子开发仿生牙科生物材料。
J Mater Chem B. 2020 Oct 14;8(38):8713-8747. doi: 10.1039/d0tb01456g. Epub 2020 Aug 4.
7
RGD-Dendrimer-Poly(L-lactic) Acid Nanopatterned Substrates for the Early Chondrogenesis of Human Mesenchymal Stromal Cells Derived from Osteoarthritic and Healthy Donors.用于源自骨关节炎和健康供体的人间充质基质细胞早期软骨形成的RGD-树枝状聚合物-聚(L-乳酸)酸纳米图案化基质
Materials (Basel). 2020 May 13;13(10):2247. doi: 10.3390/ma13102247.
8
Prechondrogenic ATDC5 Cell Attachment and Differentiation on Graphene Foam; Modulation by Surface Functionalization with Fibronectin.原代软骨前体 ATDC5 细胞在泡沫石墨烯上的黏附与分化;通过纤维连接蛋白表面功能化进行调控。
ACS Appl Mater Interfaces. 2019 Nov 13;11(45):41906-41924. doi: 10.1021/acsami.9b14670. Epub 2019 Nov 1.
9
Tissue engineering the cancer microenvironment-challenges and opportunities.癌症微环境的组织工程——挑战与机遇
Biophys Rev. 2018 Dec;10(6):1695-1711. doi: 10.1007/s12551-018-0466-8. Epub 2018 Nov 8.
10
Porous Substrates Promote Endothelial Migration at the Expense of Fibronectin Fibrillogenesis.多孔基质以牺牲纤连蛋白原纤维形成的代价促进内皮细胞迁移。
ACS Biomater Sci Eng. 2018 Jan 8;4(1):222-230. doi: 10.1021/acsbiomaterials.7b00792. Epub 2017 Nov 28.
聚丙烯酸酯侧链长度决定纤连蛋白在细胞/材料界面的迁移率。
Langmuir. 2016 Jan 26;32(3):800-9. doi: 10.1021/acs.langmuir.5b03259. Epub 2016 Jan 7.
4
Stiffening and unfolding of early deposited-fibronectin increase proangiogenic factor secretion by breast cancer-associated stromal cells.早期沉积的纤连蛋白的硬化和展开增加了乳腺癌相关基质细胞的促血管生成因子分泌。
Biomaterials. 2015 Jun;54:63-71. doi: 10.1016/j.biomaterials.2015.03.019. Epub 2015 Mar 29.
5
Modulation of endothelial cell migration via manipulation of adhesion site growth using nanopatterned surfaces.通过使用纳米图案化表面来操纵黏附部位的生长来调节内皮细胞的迁移。
ACS Appl Mater Interfaces. 2015 Feb 25;7(7):4390-400. doi: 10.1021/am508906f. Epub 2015 Feb 10.
6
A material-based platform to modulate fibronectin activity and focal adhesion assembly.一种用于调节纤连蛋白活性和粘着斑组装的基于材料的平台。
Biores Open Access. 2014 Dec 1;3(6):286-96. doi: 10.1089/biores.2014.0033.
7
The Focal Adhesion Analysis Server: a web tool for analyzing focal adhesion dynamics.黏着斑分析服务器:一种用于分析黏着斑动力学的网络工具。
F1000Res. 2013 Mar 4;2:68. doi: 10.12688/f1000research.2-68.v1. eCollection 2013.
8
Role of material-driven fibronectin fibrillogenesis in protein remodeling.物质驱动的纤连蛋白原纤维形成在蛋白质重塑中的作用。
Biores Open Access. 2013 Oct;2(5):364-73. doi: 10.1089/biores.2013.0017.
9
Predicting how cells spread and migrate: focal adhesion size does matter.预测细胞如何扩散和迁移:粘着斑大小很重要。
Cell Adh Migr. 2013 May-Jun;7(3):293-6. doi: 10.4161/cam.24804. Epub 2013 Apr 29.
10
Dynamic modeling of cell migration and spreading behaviors on fibronectin coated planar substrates and micropatterned geometries.在纤连蛋白涂覆的平面基底和微图案化结构上细胞迁移和扩展行为的动力学建模。
PLoS Comput Biol. 2013;9(2):e1002926. doi: 10.1371/journal.pcbi.1002926. Epub 2013 Feb 28.